TW555762B - Novel intermediates for the preparation of acylphosphine photoinitiator compounds, novel bisacylphosphine and monoacylphosphine compounds, process for the preparation of the same and use of said compounds - Google Patents
Novel intermediates for the preparation of acylphosphine photoinitiator compounds, novel bisacylphosphine and monoacylphosphine compounds, process for the preparation of the same and use of said compounds Download PDFInfo
- Publication number
- TW555762B TW555762B TW090102568A TW90102568A TW555762B TW 555762 B TW555762 B TW 555762B TW 090102568 A TW090102568 A TW 090102568A TW 90102568 A TW90102568 A TW 90102568A TW 555762 B TW555762 B TW 555762B
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- Prior art keywords
- lithium
- alkyl
- oxide
- chloro
- phosphine
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 186
- 238000002360 preparation method Methods 0.000 title claims abstract description 31
- 239000000543 intermediate Substances 0.000 title claims abstract description 5
- 238000000034 method Methods 0.000 title claims description 40
- 229910052744 lithium Inorganic materials 0.000 claims abstract description 174
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 108
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 84
- 150000002367 halogens Chemical class 0.000 claims abstract description 83
- 239000001257 hydrogen Substances 0.000 claims abstract description 77
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 77
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 49
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 26
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 24
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 16
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims abstract description 10
- 229910052700 potassium Inorganic materials 0.000 claims abstract description 10
- 229910052708 sodium Inorganic materials 0.000 claims abstract description 10
- -1 sulphenyl Chemical group 0.000 claims description 1514
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Natural products P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims description 396
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims description 202
- 125000000217 alkyl group Chemical group 0.000 claims description 198
- 238000011049 filling Methods 0.000 claims description 140
- 239000000203 mixture Substances 0.000 claims description 100
- 238000007254 oxidation reaction Methods 0.000 claims description 97
- 230000003647 oxidation Effects 0.000 claims description 95
- 238000000576 coating method Methods 0.000 claims description 54
- 238000006243 chemical reaction Methods 0.000 claims description 51
- 125000003545 alkoxy group Chemical group 0.000 claims description 46
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 39
- 239000007858 starting material Substances 0.000 claims description 30
- 125000003118 aryl group Chemical group 0.000 claims description 26
- 239000011248 coating agent Substances 0.000 claims description 25
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 25
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 23
- 239000000460 chlorine Substances 0.000 claims description 22
- 239000000463 material Substances 0.000 claims description 22
- 125000001624 naphthyl group Chemical group 0.000 claims description 21
- 239000004305 biphenyl Substances 0.000 claims description 20
- 235000010290 biphenyl Nutrition 0.000 claims description 20
- 239000001301 oxygen Substances 0.000 claims description 20
- 229920000642 polymer Polymers 0.000 claims description 19
- 125000003342 alkenyl group Chemical group 0.000 claims description 18
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 18
- 239000000976 ink Substances 0.000 claims description 18
- 229910052757 nitrogen Inorganic materials 0.000 claims description 18
- 238000007639 printing Methods 0.000 claims description 18
- 239000000758 substrate Substances 0.000 claims description 18
- 239000000178 monomer Substances 0.000 claims description 17
- 229920002120 photoresistant polymer Polymers 0.000 claims description 17
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 17
- 239000000654 additive Substances 0.000 claims description 15
- 229910052801 chlorine Inorganic materials 0.000 claims description 15
- 239000000843 powder Substances 0.000 claims description 15
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims description 14
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 13
- 238000007645 offset printing Methods 0.000 claims description 12
- 229910052698 phosphorus Inorganic materials 0.000 claims description 12
- 238000006467 substitution reaction Methods 0.000 claims description 12
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 11
- 125000002947 alkylene group Chemical group 0.000 claims description 11
- 125000004414 alkyl thio group Chemical group 0.000 claims description 10
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 10
- 230000003287 optical effect Effects 0.000 claims description 9
- 125000004437 phosphorous atom Chemical group 0.000 claims description 9
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 8
- 238000007650 screen-printing Methods 0.000 claims description 8
- 239000011593 sulfur Substances 0.000 claims description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 7
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 7
- 150000003003 phosphines Chemical class 0.000 claims description 7
- PXXJHWLDUBFPOL-UHFFFAOYSA-N benzamidine Chemical group NC(=N)C1=CC=CC=C1 PXXJHWLDUBFPOL-UHFFFAOYSA-N 0.000 claims description 6
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 6
- 239000000853 adhesive Substances 0.000 claims description 5
- 230000001070 adhesive effect Effects 0.000 claims description 5
- 239000002131 composite material Substances 0.000 claims description 5
- NLFBCYMMUAKCPC-KQQUZDAGSA-N ethyl (e)-3-[3-amino-2-cyano-1-[(e)-3-ethoxy-3-oxoprop-1-enyl]sulfanyl-3-oxoprop-1-enyl]sulfanylprop-2-enoate Chemical compound CCOC(=O)\C=C\SC(=C(C#N)C(N)=O)S\C=C\C(=O)OCC NLFBCYMMUAKCPC-KQQUZDAGSA-N 0.000 claims description 5
- 239000003365 glass fiber Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 230000007062 hydrolysis Effects 0.000 claims description 5
- 238000006460 hydrolysis reaction Methods 0.000 claims description 5
- REJGOFYVRVIODZ-UHFFFAOYSA-N phosphanium;chloride Chemical compound P.Cl REJGOFYVRVIODZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000005987 sulfurization reaction Methods 0.000 claims description 5
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims description 4
- 230000000694 effects Effects 0.000 claims description 4
- 238000004073 vulcanization Methods 0.000 claims description 4
- 150000004820 halides Chemical class 0.000 claims description 3
- 238000012360 testing method Methods 0.000 claims description 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
- 125000003358 C2-C20 alkenyl group Chemical group 0.000 claims description 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 2
- 230000001678 irradiating effect Effects 0.000 claims description 2
- 239000003094 microcapsule Substances 0.000 claims description 2
- 238000004806 packaging method and process Methods 0.000 claims description 2
- PCTMTFRHKVHKIS-BMFZQQSSSA-N (1s,3r,4e,6e,8e,10e,12e,14e,16e,18s,19r,20r,21s,25r,27r,30r,31r,33s,35r,37s,38r)-3-[(2r,3s,4s,5s,6r)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-19,25,27,30,31,33,35,37-octahydroxy-18,20,21-trimethyl-23-oxo-22,39-dioxabicyclo[33.3.1]nonatriaconta-4,6,8,10 Chemical compound C1C=C2C[C@@H](OS(O)(=O)=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2.O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@H](C)[C@@H](O)[C@@H](C)[C@H](C)OC(=O)C[C@H](O)C[C@H](O)CC[C@@H](O)[C@H](O)C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 PCTMTFRHKVHKIS-BMFZQQSSSA-N 0.000 claims 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
- VKEQBMCRQDSRET-UHFFFAOYSA-N Methylone Chemical group CNC(C)C(=O)C1=CC=C2OCOC2=C1 VKEQBMCRQDSRET-UHFFFAOYSA-N 0.000 claims 1
- 241000489455 Sitta europaea Species 0.000 claims 1
- 150000001555 benzenes Chemical group 0.000 claims 1
- 235000014121 butter Nutrition 0.000 claims 1
- 239000000539 dimer Substances 0.000 claims 1
- 238000000605 extraction Methods 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000001288 lysyl group Chemical group 0.000 claims 1
- 238000006053 organic reaction Methods 0.000 claims 1
- YSWYYGKGAYSAOJ-UHFFFAOYSA-N phosphane Chemical class P.P YSWYYGKGAYSAOJ-UHFFFAOYSA-N 0.000 claims 1
- XHTJLMYQJHCUPE-UHFFFAOYSA-N phosphanylphosphonic acid Chemical compound OP(O)(P)=O XHTJLMYQJHCUPE-UHFFFAOYSA-N 0.000 claims 1
- 150000003464 sulfur compounds Chemical class 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 2
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 112
- 150000002148 esters Chemical class 0.000 description 96
- 238000005481 NMR spectroscopy Methods 0.000 description 74
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 68
- 230000002079 cooperative effect Effects 0.000 description 61
- 239000000123 paper Substances 0.000 description 42
- 238000004679 31P NMR spectroscopy Methods 0.000 description 36
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 36
- 239000002585 base Substances 0.000 description 29
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 26
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 26
- 230000000875 corresponding effect Effects 0.000 description 25
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 24
- MFLDWEWCKBTVEX-UHFFFAOYSA-N lithium;phenylphosphane Chemical compound [Li].PC1=CC=CC=C1 MFLDWEWCKBTVEX-UHFFFAOYSA-N 0.000 description 23
- 150000003254 radicals Chemical class 0.000 description 21
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 20
- 125000004429 atom Chemical group 0.000 description 20
- 238000004519 manufacturing process Methods 0.000 description 19
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 18
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- 229920001577 copolymer Polymers 0.000 description 17
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- 125000004432 carbon atom Chemical group C* 0.000 description 16
- 238000002844 melting Methods 0.000 description 16
- 230000008018 melting Effects 0.000 description 16
- 239000002253 acid Substances 0.000 description 15
- RPGWZZNNEUHDAQ-UHFFFAOYSA-N phenylphosphine Chemical compound PC1=CC=CC=C1 RPGWZZNNEUHDAQ-UHFFFAOYSA-N 0.000 description 15
- 239000010410 layer Substances 0.000 description 14
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 13
- 239000012964 benzotriazole Substances 0.000 description 13
- 239000003999 initiator Substances 0.000 description 13
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 13
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 12
- 239000007983 Tris buffer Substances 0.000 description 12
- 150000001412 amines Chemical class 0.000 description 12
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 12
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 12
- 238000009472 formulation Methods 0.000 description 12
- 229910052751 metal Inorganic materials 0.000 description 12
- 239000002184 metal Substances 0.000 description 12
- 239000000049 pigment Substances 0.000 description 12
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 11
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 11
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- 239000000047 product Substances 0.000 description 11
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 10
- 238000005160 1H NMR spectroscopy Methods 0.000 description 10
- 239000004808 2-ethylhexylester Substances 0.000 description 10
- 101100167062 Caenorhabditis elegans chch-3 gene Proteins 0.000 description 10
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 10
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 10
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 10
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 10
- 229920000728 polyester Polymers 0.000 description 10
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- IPBVNPXQWQGGJP-UHFFFAOYSA-N acetic acid phenyl ester Natural products CC(=O)OC1=CC=CC=C1 IPBVNPXQWQGGJP-UHFFFAOYSA-N 0.000 description 9
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- 239000010949 copper Substances 0.000 description 9
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 9
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 9
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- WZEOZJQLTRFNCU-UHFFFAOYSA-N trifluoro(trifluoromethoxy)methane Chemical compound FC(F)(F)OC(F)(F)F WZEOZJQLTRFNCU-UHFFFAOYSA-N 0.000 description 9
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 8
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- 230000005855 radiation Effects 0.000 description 8
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 description 7
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- 101150041968 CDC13 gene Proteins 0.000 description 5
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- 125000005504 styryl group Chemical group 0.000 description 1
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- ZSSMIQURWRIOCN-UHFFFAOYSA-N tert-butyl(phenyl)phosphane Chemical compound CC(C)(C)PC1=CC=CC=C1 ZSSMIQURWRIOCN-UHFFFAOYSA-N 0.000 description 1
- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 description 1
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- 230000008719 thickening Effects 0.000 description 1
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- JFLKFZNIIQFQBS-FNCQTZNRSA-N trans,trans-1,4-Diphenyl-1,3-butadiene Chemical group C=1C=CC=CC=1\C=C\C=C\C1=CC=CC=C1 JFLKFZNIIQFQBS-FNCQTZNRSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- AYNNSCRYTDRFCP-UHFFFAOYSA-N triazene Chemical compound NN=N AYNNSCRYTDRFCP-UHFFFAOYSA-N 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- IVIIAEVMQHEPAY-UHFFFAOYSA-N tridodecyl phosphite Chemical compound CCCCCCCCCCCCOP(OCCCCCCCCCCCC)OCCCCCCCCCCCC IVIIAEVMQHEPAY-UHFFFAOYSA-N 0.000 description 1
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- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical class CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 description 1
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- 125000004953 trihalomethyl group Chemical group 0.000 description 1
- TWQULNDIKKJZPH-UHFFFAOYSA-K trilithium;phosphate Chemical compound [Li+].[Li+].[Li+].[O-]P([O-])([O-])=O TWQULNDIKKJZPH-UHFFFAOYSA-K 0.000 description 1
- VRLDDYIKZCBFEZ-UHFFFAOYSA-N trimethoxy(phenyl)phosphanium Chemical compound CO[P+](OC)(OC)C1=CC=CC=C1 VRLDDYIKZCBFEZ-UHFFFAOYSA-N 0.000 description 1
- WHAFDJWJDDPMDO-UHFFFAOYSA-N trimethyl(phenyl)phosphanium Chemical compound C[P+](C)(C)C1=CC=CC=C1 WHAFDJWJDDPMDO-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
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- WGKLOLBTFWFKOD-UHFFFAOYSA-N tris(2-nonylphenyl) phosphite Chemical compound CCCCCCCCCC1=CC=CC=C1OP(OC=1C(=CC=CC=1)CCCCCCCCC)OC1=CC=CC=C1CCCCCCCCC WGKLOLBTFWFKOD-UHFFFAOYSA-N 0.000 description 1
- XHGIFBQQEGRTPB-UHFFFAOYSA-N tris(prop-2-enyl) phosphate Chemical compound C=CCOP(=O)(OCC=C)OCC=C XHGIFBQQEGRTPB-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 229920006305 unsaturated polyester Polymers 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
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- 238000010792 warming Methods 0.000 description 1
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- 239000008096 xylene Substances 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
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- C07F9/28—Phosphorus compounds with one or more P—C bonds
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/60—Preparations for dentistry comprising organic or organo-metallic additives
- A61K6/62—Photochemical radical initiators
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
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- C07F9/02—Phosphorus compounds
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-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
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- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/5036—Phosphines containing the structure -C(=X)-P or NC-P
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
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- C07F9/5337—Phosphine oxides or thioxides containing the structure -C(=X)-P(=X) or NC-P(=X) (X = O, S, Se)
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
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- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
- C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D4/00—Coating compositions, e.g. paints, varnishes or lacquers, based on organic non-macromolecular compounds having at least one polymerisable carbon-to-carbon unsaturated bond ; Coating compositions, based on monomers of macromolecular compounds of groups C09D183/00 - C09D183/16
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- G—PHYSICS
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- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
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- G03F7/0045—Photosensitive materials with organic non-macromolecular light-sensitive compounds not otherwise provided for, e.g. dissolution inhibitors
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- G—PHYSICS
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- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/027—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds
- G03F7/028—Non-macromolecular photopolymerisable compounds having carbon-to-carbon double bonds, e.g. ethylenic compounds with photosensitivity-increasing substances, e.g. photoinitiators
- G03F7/029—Inorganic compounds; Onium compounds; Organic compounds having hetero atoms other than oxygen, nitrogen or sulfur
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- G—PHYSICS
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- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/075—Silicon-containing compounds
- G03F7/0755—Non-macromolecular compounds containing Si-O, Si-C or Si-N bonds
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
- G03F7/0384—Macromolecular compounds which are rendered insoluble or differentially wettable with ethylenic or acetylenic bands in the main chain of the photopolymer
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/004—Photosensitive materials
- G03F7/038—Macromolecular compounds which are rendered insoluble or differentially wettable
- G03F7/0388—Macromolecular compounds which are rendered insoluble or differentially wettable with ethylenic or acetylenic bands in the side chains of the photopolymer
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
- Y10S430/1055—Radiation sensitive composition or product or process of making
- Y10S430/114—Initiator containing
- Y10S430/124—Carbonyl compound containing
Landscapes
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- Health & Medical Sciences (AREA)
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- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biophysics (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Polymerisation Methods In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Materials For Photolithography (AREA)
- Printing Methods (AREA)
Applications Claiming Priority (1)
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| CH2552000 | 2000-02-08 |
Publications (1)
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| TW555762B true TW555762B (en) | 2003-10-01 |
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| TW090102568A TW555762B (en) | 2000-02-08 | 2001-02-07 | Novel intermediates for the preparation of acylphosphine photoinitiator compounds, novel bisacylphosphine and monoacylphosphine compounds, process for the preparation of the same and use of said compounds |
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| BR (1) | BR0100910A (enExample) |
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| DE (1) | DE10105046A1 (enExample) |
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| IT (1) | ITMI20010242A1 (enExample) |
| NL (1) | NL1017310C2 (enExample) |
| TW (1) | TW555762B (enExample) |
Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SK286152B6 (sk) * | 1998-11-30 | 2008-04-07 | Ciba Specialty Chemicals Holding Inc. | Spôsob prípravy acylfosfínov, acylfosfínoxidov a acylfosfínsulfidov |
| CZ297808B6 (cs) | 1999-10-20 | 2007-04-04 | Ciba Specialty Chemicals Holding Inc. | Fotoiniciacní prostredky, zpusob jejich prípravy a jejich pouzití |
| GB2365430B (en) | 2000-06-08 | 2002-08-28 | Ciba Sc Holding Ag | Acylphosphine photoinitiators and intermediates |
| AU2002223526A1 (en) * | 2000-09-14 | 2002-03-26 | Ciba Specialty Chemicals Holding Inc. | Acylphosphine oxide photoinitiators in methacrylate casting resins |
| JP4225898B2 (ja) * | 2001-08-21 | 2009-02-18 | チバ ホールディング インコーポレーテッド | 深色モノ−及びビス−アシルホスフィンオキシド及びスルフィド並びに光開始剤としてのこれらの使用 |
| BR0214324A (pt) * | 2001-11-20 | 2004-11-03 | Ciba Sc Holding Ag | Formas diméricas e multiméricas de acilfosfinas, óxidos de acilfosfina e sulfetos de acilfosfina |
| DE10206096A1 (de) * | 2002-02-13 | 2003-08-14 | Basf Ag | Mono- und Bisacylphosphinderivate |
| MXPA04011923A (es) * | 2002-06-11 | 2005-03-31 | Ciba Sc Holding Ag | Formas multimericas de oxidos de mono- y bis-acilfosfinas. |
| DE602004005981T8 (de) * | 2003-05-23 | 2008-04-30 | Ciba Specialty Chemicals Holding Inc. | Stark haftende oberflächenbeschichtungen |
| CA2531318A1 (en) * | 2003-07-18 | 2005-02-17 | Ciba Specialty Chemicals Holding Inc. | Process for preparing acylphosphanes and derivatives thereof |
| EP1699385B1 (en) | 2003-12-29 | 2012-10-24 | Abbott Medical Optics Inc. | Intraocular lenses having a visible light-selective-transmissive-region |
| US20050154109A1 (en) * | 2004-01-12 | 2005-07-14 | Minyu Li | Floor finish with lightening agent |
| US7278737B2 (en) | 2004-04-30 | 2007-10-09 | Advanced Medical Optics, Inc. | Ophthalmic devices having a highly selective violet light transmissive filter and related methods |
| US20060115516A1 (en) | 2004-11-22 | 2006-06-01 | Pearson Jason C | Copolymerizable methine and anthraquinone compounds and articles containing them |
| ATE549649T1 (de) * | 2004-11-22 | 2012-03-15 | Abbott Medical Optics Inc | Copolymerisierbare azoverbindungen und sie enthaltende gegenstände |
| JP5148283B2 (ja) * | 2004-11-23 | 2013-02-20 | チバ ホールディング インコーポレーテッド | アシルホスファン及びその誘導体の製造方法 |
| GB2422678B (en) * | 2005-01-25 | 2009-03-11 | Photocentric Ltd | Method of making a photopolymer plate |
| JP2006252787A (ja) * | 2005-03-08 | 2006-09-21 | Toppan Printing Co Ltd | 有機el素子製造方法および有機el素子 |
| JP5232365B2 (ja) * | 2005-06-01 | 2013-07-10 | 富士フイルム株式会社 | フッ素化光重合開始剤を含む光学フィルム、反射防止フィルム、偏光板、およびそれを用いた画像表示装置 |
| GB2478470B8 (en) | 2008-11-17 | 2014-05-21 | Sierra Wireless Inc | Method and apparatus for network port and netword address translation |
| US8228848B2 (en) * | 2008-11-17 | 2012-07-24 | Sierra Wireless, Inc. | Method and apparatus for facilitating push communication across a network boundary |
| US8924486B2 (en) * | 2009-02-12 | 2014-12-30 | Sierra Wireless, Inc. | Method and system for aggregating communications |
| CN102405239B (zh) | 2009-04-20 | 2014-10-15 | 瑞士联邦苏黎世技术大学 | 聚合物纳米颗粒 |
| US8633258B2 (en) | 2010-06-30 | 2014-01-21 | Dsm Ip Assets B.V. | D1492 liquid BAPO photoinitiator and its use in radiation curable compositions |
| WO2012106820A1 (en) | 2011-02-08 | 2012-08-16 | Sierra Wireless, Inc. | Method and system for forwarding data between network devices |
| DE102012212429A1 (de) | 2012-07-16 | 2014-01-16 | Voco Gmbh | Dentalhandgerät, Verfahren und Verwendung desselben zum Aushärten lichthärtbaren Materials |
| GB201213163D0 (en) * | 2012-07-24 | 2012-09-05 | Lambson Ltd | Photopolymerisation processes and novel compounds therefor |
| WO2014053455A1 (en) * | 2012-10-01 | 2014-04-10 | ETH Zürich | A process for the preparation of acylphosphanes |
| WO2014097079A1 (en) | 2012-12-18 | 2014-06-26 | Basf Se | Semiconducting materials based on naphthalenediimide-vinylene-oligothiophene-vinylene polymers |
| CN110845530A (zh) * | 2012-12-19 | 2020-02-28 | Igm集团公司 | 双酰基次膦酸的衍生物、其制备及其作为光敏引发剂的用途 |
| CN108779192B (zh) * | 2016-01-11 | 2021-01-26 | 汉高知识产权控股有限责任公司 | 有机硅相容的化合物 |
| EP3409680B1 (en) * | 2017-05-30 | 2021-01-06 | IGM Group B.V. | Synthesis of bis(acyl)phosphines by activation of unreactive metal phosphides |
| CN107082787B (zh) * | 2017-06-09 | 2019-05-17 | 江苏富比亚化学品有限公司 | 一种苯甲酰基苯基次膦酸及其衍生物的制备方法 |
| TWI782066B (zh) | 2017-08-03 | 2022-11-01 | 德商漢高股份有限及兩合公司 | 可固化的聚矽氧光學透明黏著劑及其用途 |
| WO2019037016A1 (en) * | 2017-08-24 | 2019-02-28 | Henkel IP & Holding GmbH | SILICONE POLYMER PHOTO-INITIATOR AND USES THEREOF |
| KR20200100610A (ko) | 2017-12-27 | 2020-08-26 | 헨켈 아이피 앤드 홀딩 게엠베하 | 광학적으로 투명한 감압성 접착제 및 그의 용도 |
| CN112654629B (zh) * | 2018-10-01 | 2024-06-14 | 陶氏东丽株式会社 | 有机硅化合物、制备方法及其用途 |
| EP4149758A4 (en) * | 2020-05-14 | 2024-09-11 | 3M Innovative Properties Company | MULTILAYER OPTICAL FILMS COMPRISING AT LEAST ONE LAYER OF FLUORINATED (CO)POLYMER PREPARED USING A FLUORINATED PHOTOINITIATOR, AND METHODS OF PREPARATION AND USE THEREOF |
| KR102651787B1 (ko) * | 2021-07-14 | 2024-03-26 | 주식회사 엘지에너지솔루션 | 리튬 이차전지용 비수계 전해액 및 이를 포함하는 리튬 이차전지 |
| CN114349788B (zh) * | 2021-12-30 | 2023-06-20 | 华南理工大学 | 一种光引发剂及其制备方法与应用 |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2830928A1 (de) * | 1978-07-14 | 1980-01-31 | Basf Ag | Lichthaertbare form-, traenk- und ueberzugsmassen |
| DE3020092A1 (de) * | 1980-05-27 | 1981-12-10 | Basf Ag, 6700 Ludwigshafen | Acylphosphinverbindungen und ihre verwendung |
| DE3114341A1 (de) * | 1981-04-09 | 1982-11-11 | Basf Ag, 6700 Ludwigshafen | Acylphosphinverbindungen, ihre herstellung und verwendung |
| DE3133419A1 (de) * | 1981-08-24 | 1983-03-10 | Basf Ag, 6700 Ludwigshafen | Acylphosphinoxidverbindungen und ihre verwendung |
| DE3443221A1 (de) * | 1984-11-27 | 1986-06-05 | ESPE Fabrik pharmazeutischer Präparate GmbH, 8031 Seefeld | Bisacylphosphinoxide, ihre herstellung und verwendung |
| US4985472A (en) * | 1987-05-01 | 1991-01-15 | Mitsubishi Rayon Company, Ltd. | Actinic ray curable composition for casting polymerization and casting polymerization molded products |
| JPH01309001A (ja) * | 1988-02-15 | 1989-12-13 | Mitsubishi Rayon Co Ltd | プラスチックレンズ材料 |
| US5218009A (en) | 1989-08-04 | 1993-06-08 | Ciba-Geigy Corporation | Mono- and di-acylphosphine oxides |
| ES2098260T3 (es) * | 1989-08-04 | 1997-05-01 | Ciba Geigy Ag | Oxidos de mono- y diacilfosfina. |
| RU2091385C1 (ru) | 1991-09-23 | 1997-09-27 | Циба-Гейги АГ | Бисацилфосфиноксиды, состав и способ нанесения покрытий |
| DE4230555A1 (de) * | 1992-09-12 | 1994-03-17 | Basf Ag | Verfahren zur Herstellung von alpha-Carbonylphosphinoxiden |
| EP0662991A1 (en) * | 1992-09-30 | 1995-07-19 | Ppg Industries, Inc. | Pigmented compositions and methods for producing radiation curable coatings of very low gloss |
| ZA941879B (en) * | 1993-03-18 | 1994-09-19 | Ciba Geigy | Curing compositions containing bisacylphosphine oxide photoinitiators |
| TW381106B (en) * | 1994-09-02 | 2000-02-01 | Ciba Sc Holding Ag | Alkoxyphenyl-substituted bisacylphosphine oxides |
| CH691970A5 (de) * | 1996-03-04 | 2001-12-14 | Ciba Sc Holding Ag | Alkylphenylbisacylphosphinoxide und Photoinitiatormischungen. |
| JPH09241312A (ja) * | 1996-03-08 | 1997-09-16 | Showa Denko Kk | 光硬化性人造大理石用組成物及びその硬化方法 |
| SK286152B6 (sk) | 1998-11-30 | 2008-04-07 | Ciba Specialty Chemicals Holding Inc. | Spôsob prípravy acylfosfínov, acylfosfínoxidov a acylfosfínsulfidov |
| SE9904080D0 (sv) * | 1998-12-03 | 1999-11-11 | Ciba Sc Holding Ag | Fotoinitiatorberedning |
| SG98433A1 (en) * | 1999-12-21 | 2003-09-19 | Ciba Sc Holding Ag | Iodonium salts as latent acid donors |
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2001
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- 2001-02-05 US US09/776,657 patent/US6399805B2/en not_active Expired - Fee Related
- 2001-02-05 DE DE10105046A patent/DE10105046A1/de not_active Withdrawn
- 2001-02-06 CA CA002334291A patent/CA2334291A1/en not_active Abandoned
- 2001-02-06 BE BE2001/0087A patent/BE1013960A3/fr not_active IP Right Cessation
- 2001-02-07 CN CNB011034874A patent/CN1200943C/zh not_active Expired - Fee Related
- 2001-02-07 FR FR0101630A patent/FR2804683B1/fr not_active Expired - Fee Related
- 2001-02-07 KR KR1020010005813A patent/KR100769838B1/ko not_active Expired - Fee Related
- 2001-02-07 TW TW090102568A patent/TW555762B/zh not_active IP Right Cessation
- 2001-02-07 ES ES200100276A patent/ES2195706B1/es not_active Expired - Fee Related
- 2001-02-07 IT IT2001MI000242A patent/ITMI20010242A1/it unknown
- 2001-02-08 NL NL1017310A patent/NL1017310C2/nl not_active IP Right Cessation
- 2001-02-08 BR BR0100910-9A patent/BR0100910A/pt not_active Application Discontinuation
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- 2001-10-22 US US10/037,111 patent/US6579663B2/en not_active Expired - Fee Related
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2011
- 2011-04-19 JP JP2011093335A patent/JP2011140524A/ja active Pending
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| US20020107413A1 (en) | 2002-08-08 |
| US6579663B2 (en) | 2003-06-17 |
| ES2195706B1 (es) | 2005-03-01 |
| NL1017310C2 (nl) | 2002-06-18 |
| GB2360283B (en) | 2002-08-21 |
| CN1200943C (zh) | 2005-05-11 |
| US20010031898A1 (en) | 2001-10-18 |
| NL1017310A1 (nl) | 2001-08-09 |
| KR100769838B1 (ko) | 2007-10-24 |
| GB2360283A (en) | 2001-09-19 |
| JP2011140524A (ja) | 2011-07-21 |
| BE1013960A3 (fr) | 2003-01-14 |
| KR20010083161A (ko) | 2001-08-31 |
| CA2334291A1 (en) | 2001-08-08 |
| FR2804683B1 (fr) | 2005-04-08 |
| FR2804683A1 (fr) | 2001-08-10 |
| DE10105046A1 (de) | 2001-08-09 |
| GB0102398D0 (en) | 2001-03-14 |
| ITMI20010242A1 (it) | 2002-08-07 |
| CN1308081A (zh) | 2001-08-15 |
| JP2001270894A (ja) | 2001-10-02 |
| BR0100910A (pt) | 2001-10-02 |
| ES2195706A1 (es) | 2003-12-01 |
| US6399805B2 (en) | 2002-06-04 |
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